Job Description

Main Purpose of Role:

• Maintenance of the NB 1639 medical device internal quality management system.

• Managing of daily QA tasks:

- Updating and maintenance of documents under the MDD, MDR and IVDR scheme,
- Management the IF database,
- Collaboration on generic scheme documents,
- Publishing of documents on the SGS website,
- Bizzmine (Quality Management System); user communication and maintenance.

This role will report to the Quality & Regulatory Manager, Business Assurance.

It is remote based, and we are open to candidates located everywhere across Europe. But they must hold a valid work permit for their country of residency.

Key Accountabilities:

• Management of complaints, compliance queries and appeals,

• Management of continual improvement,

• Management of document control and records,





• Perform quality assurance check on updated quality management system documents,

• Release of updated quality management system documents in Bizzmine,

• Build a good working relationship with the Global Medical Device Certification / Competency /

Technical and Clinical Manager(s), and other Global Medical Device Team members,

• Undertake personal professional development and ensure appropriate training records are

updated,

• Provide technical support to all parts of the business,

• Maintain a full knowledge and understanding of SGS procedures, regulations, guidance

documents (e.g., MDCG) and external approval criteria,

• Support the development and maintenance of combined scheme documents.

📌 Quality Assurance Officer (1 year maternity cover) (Milano)
🏢 Sgs
📍 Milano